@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion
a
np:Assertion
.
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance
a
np:Provenance
.
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion
{
miriam-gene:10915
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN1d051305d0c6582f2a694d8b169e155f
sio:SIO_000628
miriam-gene:10915
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_provenance
{
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_assertion
dcterms:description
"[To identify the genetic modifier(s) that might alter the age at onset in Huntington's disease (HD) we have analyzed variations in GluR6 kainate receptor (GluR6), CA150 gene, Delta2642 and polymorphic CCG repeat variation in huntingtin (htt) gene in 77 HD patients and normal individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:12821179
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP697507.RAPNZR3oDoDDc9z3LOCFWQAOTY26k2TH32U6lw2fOz0UU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
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"v2.1.0" .
}